Department of Urology, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
BJU Int. 2012 Jul;110(2):211-6. doi: 10.1111/j.1464-410X.2011.10666.x. Epub 2011 Nov 16.
Study Type - Therapy (case series). Level of Evidence 4. What's known on the subject? and What does the study add? For patients electing surgical treatment, the question of the effect of surgical delay on clinical outcomes in prostate cancer is controversial. In this study we examined the effect of delay from diagnosis to surgery on outcomes in men with localized prostate cancer and found no association between time to surgery and risk of biochemical recurrence, even for patients with longer delays and high-risk disease. Men with localized prostate cancer can be reassured that reasonable delays in treatment will not influence disease outcomes.
• To examine the effect of time from last positive biopsy to surgery on clinical outcomes in men with localized prostate cancer undergoing radical prostatectomy (RP).
• We conducted a retrospective review of 2739 men who underwent RP between 1990 and 2009 at our institution. • Clinical and pathological features were compared between men undergoing RP ≤ 60, 61-90 and >90 days from the time of prostate biopsy. • A Cox proportional hazards model was used to analyse the association between clinical features and surgical delay with biochemical progression. Biochemical recurrence (BCR)-free rates were assessed using the Kaplan-Meier method.
• Of the 1568 men meeting the inclusion criteria, 1098 (70%), 303 (19.3%) and 167 (10.7%) had a delay of ≤ 60, 61-90 and >90 days, respectively, between biopsy and RP. A delay of >60 days was not associated with adverse pathological findings at surgery. • The 5-year survival rate was similar among the three groups (78-85%, P= 0.11). • In a multivariate Cox model, men with higher PSA levels, clinical stages, Gleason sums, and those of African-American race were all at higher risk for developing BCR. • A delay to surgery of >60 days was not associated with worse biochemical outcomes in a univariate and multivariate model.
• A delay of >60 days is not associated with adverse pathological outcomes in men with localized prostate cancer, nor does it correlate with worse BCR-free survival. • Patients can be assured that delaying treatment while considering therapeutic options will not adversely affect their outcomes.
• 研究从最后一次前列腺活检到手术的时间对接受根治性前列腺切除术 (RP) 的局限性前列腺癌男性临床结局的影响。
• 我们对 1990 年至 2009 年期间在我院接受 RP 的 2739 名男性进行了回顾性研究。• 将 RP 后≤60、61-90 和>90 天的男性的临床和病理特征进行比较。• 使用 Cox 比例风险模型分析临床特征和手术延迟与生化进展之间的关联。使用 Kaplan-Meier 方法评估生化复发 (BCR) 无进展率。
• 在符合纳入标准的 1568 名男性中,1098 名 (70%)、303 名 (19.3%)和 167 名 (10.7%)的前列腺活检与 RP 之间的延迟时间分别≤60、61-90 和>90 天。延迟>60 天与手术时的不良病理发现无关。• 三组的 5 年生存率相似 (78-85%,P=0.11)。• 在多变量 Cox 模型中,PSA 水平较高、临床分期较高、Gleason 总和较高以及非裔美国人的男性发生 BCR 的风险更高。• 在单变量和多变量模型中,手术延迟>60 天与生化结果较差无关。
• 延迟>60 天与局限性前列腺癌男性的不良病理结果无关,也与较差的 BCR 无复发生存率无关。• 可以向患者保证,在考虑治疗选择时延迟治疗不会对其结果产生不利影响。